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从……提取的基因组DNA通过抑制Toll样受体(TLR)介导的丝裂原活化蛋白激酶(MAPK)和核因子κB(NF-κB)信号通路减轻脂多糖(LPS)诱导的炎症反应。

Genomic DNA Extracted from Attenuates Lipopolysaccharide (LPS)-Induced Inflammatory Responses via Suppression of Toll-Like Receptor (TLR)-Mediated Mitogen-Activated Protein Kinase (MAPK) and Nuclear Factor-κB (NF-κB) Signaling Pathways.

作者信息

Choi Young Hyeon, Kim Bong Sun, Kang Seok-Seong

机构信息

Department of Food Science and Biotechnology, College of Life Science and Biotechnology, Dongguk University, Goyang 10326, Korea.

Division of Applied Food System, Major in Food Science & Technology, Seoul Women's University, Seoul 01797, Korea.

出版信息

Food Sci Anim Resour. 2023 Sep;43(5):938-947. doi: 10.5851/kosfa.2023.e43. Epub 2023 Sep 1.

Abstract

In the present study, we aimed to examine the inhibition of genomic DNA from (LpDNA) on lipopolysaccharide (PgLPS)-induced inflammatory responses in RAW264.7 cells. Pretreatment with LpDNA for 15 h significantly inhibited PgLPS-induced mRNA expression and protein secretion of interleukin (IL)-1β, IL-6, and monocyte chemoattractant protein-1. LpDNA pretreatment also reduced the mRNA expression of Toll-like receptor (TLR)2 and TLR4. Furthermore, LpDNA inhibited the phosphorylation of mitogen-activated protein kinases (MAPKs) and the activation of nuclear factor-κB (NF-κB) induced by PgLPS. Taken together, these findings demonstrate that LpDNA attenuates PgLPS-induced inflammatory responses by regulating MAPKs and NF-κB signaling pathways through the suppression of TLR2 and TLR4 expression.

摘要

在本研究中,我们旨在检测来自[具体来源未提及]的基因组DNA(LpDNA)对脂多糖(PgLPS)诱导的RAW264.7细胞炎症反应的抑制作用。用LpDNA预处理15小时可显著抑制PgLPS诱导的白细胞介素(IL)-1β、IL-6和单核细胞趋化蛋白-1的mRNA表达及蛋白分泌。LpDNA预处理还降低了Toll样受体(TLR)2和TLR4的mRNA表达。此外,LpDNA抑制了PgLPS诱导的丝裂原活化蛋白激酶(MAPKs)磷酸化及核因子-κB(NF-κB)激活。综上所述,这些发现表明LpDNA通过抑制TLR2和TLR4表达来调节MAPKs和NF-κB信号通路,从而减轻PgLPS诱导的炎症反应。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5ae0/10493568/a1730c95416d/kosfa-43-5-938-g1.jpg

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